A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022232



Internal ID18764766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12326552..12643876hg38UCSC Ensembl
Innerchr9:12326552..12643876hg19UCSC Ensembl
Innerchr9:12316552..12633876hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38317325
hg19317325
hg18317325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690588
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022232
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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